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rs876660771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 5 Hereditary diffuse gastric cancer
(G;G) 0 common in clinvar


Make rs876660771(A;A)
is asnp
is mentioned by
dbSNPrs876660771
ebirs876660771
HLIrs876660771
Exacrs876660771
Varsomers876660771
Maprs876660771
PheGenIrs876660771
hapmaprs876660771
1000 genomesrs876660771
hgdprs876660771
ensemblrs876660771
gopubmedrs876660771
geneviewrs876660771
scholarrs876660771
googlers876660771
pharmgkbrs876660771
gwascentralrs876660771
openSNPrs876660771
23andMers876660771
23andMe allrs876660771
SNP Nexus

SNPshotrs876660771
SNPdbers876660771
MSV3drs876660771
GWAS Ctlgrs876660771
Max Magnitude5

Also known as c.1137+1G>A, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk rs876660771(A;A)
Alt rs876660771(A;A)
Reference rs876660771(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Hereditary diffuse gastric cancer
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Hereditary diffuse gastric cancer
Reversed 0
HGVS NC_000016.9:g.68846167G>A
CLNSRC
CLNACC RCV000219632.1, RCV000230827.1,